ID: 302 | annexin A2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (60347151..60397986, complement) | ANX2, ANX2L4, CAL1H, HEL-S-270, LIP2, LPC2, LPC2D, P36, PAP-IV | 151740 |
ID: 123283 | threonyl-tRNA synthetase 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (101653596..101724473, complement) | TARSL2, ThrRS-L | |
ID: 5464 | inorganic pyrophosphatase 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (70202835..70233429, complement) | HEL-S-66p, IOPPP, PP, PP1, SID6-8061 | 179030 |
ID: 5428 | DNA polymerase gamma, catalytic subunit [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89316320..89334824, complement) | MDP1, MIRAS, MTDPS4A, MTDPS4B, PEO1, POLGA, SANDO, SCAE, POLG | 174763 |
ID: 64423 | inverted formin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104689618..104722535) | C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 | 610982 |
ID: 6468 | F-box and WD repeat domain containing 4 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (101610666..101695295, complement) | DAC, FBW4, FBWD4, SHFM3, SHSF3 | 608071 |
ID: 81567 | thioredoxin domain containing 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7881517..7910788, complement) | ENDOPDI, ERP46, HCC-2, HCC2, PDIA15, STRF8, UNQ364 | 616412 |
ID: 389 | ras homolog family member C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (112701131..112707408, complement) | ARH9, ARHC, H9, RHOH9 | 165380 |
ID: 50628 | gem nuclear organelle associated protein 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (744421..754410, complement) | HC56, HCAP1, HHRF-1, NEDMCR, p97 | 606969 |
ID: 51380 | cysteine sulfinic acid decarboxylase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53157663..53181351, complement) | CSD, PCAP | 616569 |
ID: 7597 | zinc finger and BTB domain containing 25 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64449106..64505213, complement) | C14orf51, KUP, ZNF46 | 194541 |
ID: 138639 | protein tyrosine phosphatase domain containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94030813..94109856) | PTP9Q22 | |
ID: 30844 | EH domain containing 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (41895933..41972557, complement) | PAST4 | 605892 |
ID: 144811 | laccase domain containing 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (43879178..43893932) | C13orf31, FAMIN, JUVAR | 613409 |
ID: 9813 | EF-hand calcium binding domain 14 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (46675159..46719114, complement) | KIAA0494 | 619559 |
ID: 84062 | dystrobrevin binding protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (15522807..15663058, complement) | BLOC1S8, DBND, HPS7, My031, SDY | 607145 |
ID: 2935 | G1 to S phase transition 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11868128..11916654, complement) | 551G9.2, ETF3A, GST1, eRF3a | 139259 |
ID: 5264 | phytanoyl-CoA 2-hydroxylase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (13277799..13300064, complement) | LN1, LNAP1, PAHX1, RD, PHYH | 602026 |
ID: 657 | bone morphogenetic protein receptor type 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86755763..86932844) | 10q23del, ACVRLK3, ALK-3, ALK3, BMPR-1A, CD292, SKR5 | 601299 |
ID: 159371 | solute carrier family 35 member G1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (93893978..93909830) | C10orf60, POST, TMEM20 | 617167 |